IP Library Granted Patent US 6,989,357
Granted Patent B2
US 6,989,357 · App. 10/826,580 · Granted Jan 24, 2006

Alcohol absorbed polyalphaolefin drag reducing agents

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Quick Facts
Patent No.
US 6,989,357
App. No.
10/826,580
Granted
Jan 24, 2006
Kind
B2
Abstract

A composition including an alcohol absorbed polyalphaolefin that functions as a drag reducing agent and a process for the preparation of the drag reducing agent are disclosed. The process includes the steps of contacting alpha olefin monomers with at least one catalyst in a reactant mixture to form a polyalphaolefin. The polyalphaolefin is then contacted with at least one water insoluble alcohol for a period of time to provide an alcohol absorbed polyalphaolefin that is used as an improved drag reducing agent. Processes for reducing drag in a conduit are also disclosed.

Claims (30)

1. A process for forming a drag reducing agent, the process comprising:

contacting an alpha olefin monomer with at least one catalyst in a reactant mixture;

polymerizing the alpha olefin monomer, wherein during the polymerization at least a portion of the alpha olefin monomer polymerize in the reactant mixture to provide an ultra-high molecular weight polyalphaolefin;

cryogrinding the ultra-high molecular weight polyalphaolefin to form a cryoground polyalphaolefin having a cryoground polyalphaolefin weight; and

contacting the cryoground polyalphaolefin with at least one water insoluble alcohol for a period of time and at a temperature sufficient to form an alcohol absorbed polyalphaolefin having an alcohol absorbed polyalphaolefin weight that is at least 0.5% greater than the polyalphaolefin weight.

2. The process of claim 1 , wherein the at least one alcohol is selected from the group consisting of 1-pentanol, 1-hexanol, 1-heptanol, n-octyl alcohol, n-nonyl alcohol, 1-decanol, and mixtures thereof.

3. The process of claim 2 , wherein the period of time is at least one hour and the temperature is at least 10° C.

4. The process of claim 2 , wherein the period of time is at least seven days and the temperature is at least 20° C.

5. The process of claim 2 , wherein the period of time is at least twenty eight days and the temperature is at least 20° C.

6. The process of claim 1 , wherein the at least one alcohol is 1-pentanol.

7. The process of claim 1 , wherein the at least one alcohol is 1-hexanol.

8. The process of claim 1 , wherein the at least one alcohol is 1-heptanol.

9. The process of claim 1 , wherein the at least one alcohol is n-octyl alcohol.

10. The process of claim 1 , wherein the at least one alcohol is n-nonyl alcohol.

11. The process of claim 1 , wherein the at least one alcohol is 1-decanol.

12. A drag reducing agent comprising an alcohol absorbed polyalphaolefin, the alcohol absorbed polyalphaolefin including a cryoground polyalphaolefin having a cryoground polyalphaolefin weight and a water insoluble alcohol, wherein the alcohol absorbed polyalphaolefin includes an alcohol absorbed polyalphaolefin weight that is at least 0.5% greater than the cryoground polyalphaolefin weight.

13. The drag reducing agent of claim 12 , wherein the at least one alcohol is selected from the group consisting of 1-pentanol, 1-hexanol, 1-heptanol, n-octyl alcohol, n-nonyl alcohol, 1-decanol, and mixtures thereof.

14. The drag reducing agent of claim 12 , wherein the at least one alcohol is 1-pentanol.

15. The drag reducing agent of claim 12 , wherein the at least one alcohol is 1-hexanol.

16. The drag reducing agent of claim 12 , wherein the at least one alcohol is 1-heptanol.

17. The drag reducing agent of claim 12 , wherein the at least one alcohol is n-octyl alcohol.

18. The drag reducing agent of claim 12 , wherein the at least one alcohol is n-nonyl alcohol.

19. The drag reducing agent of claim 12 , wherein the at least one alcohol is 1-decanol.

20. A process for reducing drag in a conduit, comprising:

forming a drag reducing agent comprising an alcohol absorbed polyalphaolefin, wherein the alcohol absorbed polyalphaolefin is formed by

contacting an alpha olefin monomer with at least one catalyst in a reactant mixture,

polymerizing the alpha olefin monomer, wherein during the polymerization at least a portion of the alpha olefin monomer polymerize in the reactant mixture to provide an ultra-high molecular weight polyalphaolefin,

cryogrinding the ultra-high molecular weight polyalphaolefin to form a cryoground polyalphaolefin having a cryoground polyalphaolefin weight, and

contacting the cryoground polyalphaolefin with at least one water insoluble alcohol to form an alcohol absorbed polyalphaolefin having an alcohol absorbed polyalphaolefin weight that is at least 0.5% greater than the cryoground polyalphaolefin weight; and

introducing the alcohol absorbed polyalphaolefin into the conduit.

Assignments (13)
RELEASE OF SECURITY INTEREST Recorded Jul 6, 2022
From: JPMORGAN CHASE BANK, N.A.
To: CABOT MICROELECTRONICS CORPORATION; QED TECHNOLOGIES INTERNATIONAL, INC.; FLOWCHEM LLC; KMG ELECTRONIC CHEMICALS, INC.; KMG-BERNUTH, INC.; MPOWER SPECIALTY CHEMICALS LLC; SEALWELD (USA), INC.; INTERNATIONAL TEST SOLUTIONS, LLC; CMC MATERIALS, INC.
Reel/Frame 060592/0260 →
CHANGE OF NAME Recorded Jan 13, 2021
From: CABOT MICROELECTRONICS CORPORATION
To: CMC MATERIALS, INC.
Reel/Frame 054980/0681 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 6, 2020
From: MPOWER SPECIALTY CHEMICALS, LLC
To: CABOT MICROELECTRONICS CORPORATION
Reel/Frame 052042/0825 →
SECURITY AGREEMENT Recorded Nov 16, 2018
From: CABOT MICROELECTRONICS CORPORATION; QED TECHNOLOGIES INTERNATIONAL, INC.; FLOWCHEM LLC; KMG ELECTRONIC CHEMICALS, INC.; MPOWER SPECIALTY CHEMICALS LLC
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 047588/0263 →
RELEASE OF SECURITY INTEREST Recorded Jun 19, 2017
From: KAYNE ANDERSON SENIOR CREDIT ADVISORS, LLC, AS ADMINISTRATIVE AGENT
To: MPOWER SPECIALTY CHEMICALS LLC
Reel/Frame 042752/0261 →
SECURITY AGREEMENT Recorded Dec 6, 2013
From: MPOWER SPECIALTY CHEMICALS LLC
To: KAYNE ANDERSON SENIOR CREDIT ADVISORS, LLC, AS ADMINISTRATIVE AGENT
Reel/Frame 031768/0340 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 29, 2013
From: EATON, GERALD B; EBERT, ALAN K.
To: MPOWER SPECIALTY CHEMICALS, LLC
Reel/Frame 031502/0857 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 26, 2013
From: RE CHEM HOLDING AG
To: MONARCH ASSURANCE PLC
Reel/Frame 030295/0839 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 26, 2013
From: BETA TECHNOLOGIE AG
To: RE CHEM HOLDING AG
Reel/Frame 030294/0671 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 26, 2013
From: MONARCH ASSURANCE PLC
To: MPOWER SPECIALTY CHEMICALS LLC
Reel/Frame 030297/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 22, 2006
From: ZENITH ENERGY INTERNATIONAL CORP., LTD.
To: BETA TECHNOLOGIE AG
Reel/Frame 018616/0225 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 16, 2006
From: ADSAVAVICHAIROT, LALITA
To: ZENITH ENERGY INTERNATIONAL CORP. LTD.
Reel/Frame 018407/0669 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 5, 2006
From: ENERGY & ENVIRONMENTAL INTERNATIONAL, L.C.
To: ADSAVAVICHAIROT, LALITA
Reel/Frame 018231/0387 →